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Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building

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Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building
Androstenedione Basic Info.
Product Name: Androstenedione
Synonyms: 4-Androstenedione;4AD;3,17-Dioxoandrost-4-Ene;delta-(sup4)-Androsten-3,17-dione;delta(Sup4)-Androstene-3,17-dione;delta4-androsten-3,17-dione;delta-4-androstenedione;SKF 2170;skf2170;4-AD
CAS: 63-05-8
MF: C19H26O2
MW: 286.41
EINECS: 200-554-5
Purity: 98.88%
Manufacturer: Kafen
Characters: Near white crystalline powder, soluble in ethanol, insoluble in water
Androstenedione Applications:
Testo-ster-one precursor and metabolite with androgenic activity. Controlled substance (anabolic steroid); Simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisterone, testosterone propionate in the middle body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation.
Androstenedione Description:
4-Androstenedione can be synthesized in one of two ways. The primary pathway involves conversion of 17-hydroxypregnenolone to dehydroepiandrosterone by way of 17,20-lyase, with subsequent conversion of dehydroepiandrosterone to 4-Androstenedione via the enzyme 3-β-hydroxysteroid dehydrogenase. The secondary pathway involves conversion of 17-hydroxyprogesterone, most often a precursor to cortisol, to 4-androstenedione directly by way of 17,20-lyase. Thus, 17,20-lyase is required for the synthesis of 4-androstenedione, whether immediately or one step removed.  
The production of adrenal 4-Androstenedione is governed by ACTH, whereas production of gonadal 4-Androstenedione is under control by gonadotropins. In premenopausal women, the adrenal glands and ovaries each produce about half of the total 4-androstenedione(about 3 mg/day). After menopause, 4-androstenedione production is about halved, due primarily to the reduction of the steroid secreted by the ovary. Nevertheless, 4-androstenedione is the principal steroid produced by the postmenopausal.

Manufacturer Terlipressin Acetate With High Quality 14636-12-5

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Manufacturer Terlipressin Acetate With High Quality 14636-12-5
Terlipressin Acetate Basic Info.:
Product Name: Terlipressin Acetate
Synonyms: Terlipressin;Terlipressin Acetate;Terilipressin;
CAS: 14636-12-5
MF: C52H74N16O15S2
MW: 1227.37
EINECS: 238-680-8
Product Categories: Amino Acid Derivatives;Peptide;hormones
Usage: Terlipressin is an analogue of vasopressin used as a vasoactive drug in the management of hypotension. Terlipressin is used norepinephrine-resistant septic shock and hepatorenal syndrome. Terlipressin is also used in the treatment of acute variceal bleeding.
Terlipressin Acetate Pharmacological Effects:
Terlipressin is a novel long-acting synthetic vasopressin reagent,its chemical name is three glycyl lysine vasopressin, it is a prodrug, itself has no activity ,in vivo  , it removes three glycyl residues in its N-terminus by aminopeptidase, and slowly "releases" the active lysine vasopressin. It is this "slow release" mechanism that makes it maintain the smooth muscle contraction up to 10 hours after a single administration, whereas the same dose of vasopressin, it can maintain its activity for 20-40 minutes. On the other hand,because of the slow digestion,  lysine vasopressin in the circulation cannot reach toxic levels, and usage of  terlipressin is safer.
Pharmacological effect of terlipressin is splanchnic vascular smooth muscle contraction, and reduction of visceral blood flow (such as reducing blood flow in the mesentery, spleen, uterus, etc.), thereby reducing portal vein blood flow,and reducing portal pressure, on the other hand it may also reduce plasma renin concentration, thereby increasing the renal blood flow in patients with hepatorenal syndrome, to improve kidney function, and increase urine output. Terlipressin is currently the only drug which is able to increase mortality in patients with esophageal varices bleeding , it is previously mainly used in clinical for the treatment of variceal bleeding, in addition,terlipressin now has also been successfully used for liver and kidney integrated syndrome and refractory shock, it is also likely to play a useful role in the cardiopulmonary resuscitation . Compared with vasopressin, it has a lasting effect, and it does not cause dangerous complications, including promoting  fibrinolysis and severe complications in the cardiovascular systems, and the use of it is simple (available intravenous injection), it is more suitable for rescue and treatment of emergent and critical  patients.
Terlipressin Acetate Mechanism of Action:
Terlipressin, a synthetic triglycyl-lysine derivative of vasopressin, is a inactive prodrug. It has pressor and antidiuretic effects. Following IV injection, lysine vasopressin are released following the enzymatic cleavage of 3 glycyl moieties.
Duration: 4-6 hr.

N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-imino-2-phenazinamine 95%

Name   N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-imino-2-phenazinamine
Synonyms   B 628; B 628 (pharmaceutical)
Molecular Structure   CAS # 102262-55-5, N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-imino-2-phenazinamine, B 628, B 628 (pharmaceutical)
Molecular Formula   C24H16Cl2N4
Molecular Weight   431.32
CAS Registry Number   102262-55-5


Raw Material Telmisartan For Anti-cancer Agent CAS 144701-48-4

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Raw Material Telmisartan For Anti-cancer Agent CAS 144701-48-4
Telmisartan Basic Info.:
Product Name: Telmisartan
CAS: 144701-48-4
MF: C33H30N4O2
MW: 514.63
MP: 261-263°C
Purity: 99%
Density: 1.16
Storage temp.: Hygroscopic, -20°C Freezer, Under Inert Atmosphere
Solubility DMSO: >5 mg/mL at 60 °C
Water Solubility: insoluble
Chemical Properties: White or off white crystalline powder
Usage: An angiotensin II receptor antagonist.API.
Medical Use Of Telmisartan:
Telmisartan is a new antihypertensive drugs, a specific angiotensin Ⅱ receptor (AT1 type) antagonist. Telmisartan alternative angiotensin Ⅱ receptor binding with high affinity AT1 receptor subtype. Telmisartan AT1 receptor sites in any part of agonist effects of telmisartan in combination with selective AT1 receptors, the binding lasting effect. Buck stability does not cause coughing.

White Ghrp-2 Human Growth Hormone For Bodybuilding 158861-67-7

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White Ghrp-2 Human Growth Hormone For Bodybuilding 158861-67-7
GHRP 2 Basic Info.:
Product name: GHRP-2 (GHRP-2 Acetate )
Synonym: Pralmorelin; GHRP2; D-Alanyl-3-(2-naphthalenyl)-D-alanyl-L-alanyl-L-tryptophyl-D-phenylalanyl-L-lysinamide; GHRP 2; 
CAS: 158861-67-7
MF: C45H55N9O6
MW: 817.9749
Purity: 98%
Appearance: White powder
Density: 1.27g/cm3
Boiling point: 1265.3°C at 760 mmHg
Flashing point: 719°C
Function: To stimulate GH secretion, appetite, and to gain weight
GHRP 2 Description:
GHRP-2 is a synthetic agonist of ghrelin, the newly-discovered gut peptide which binds to the GH secretagogue receptor. Ghrelin has two major effects, stimulating both GH secretion and appetite/meal initiation. GHRP-2 has been extensively studied for its utility as a GHS. Since the test subjects body will end up producing more GH this way, fat will be reduced while lean muscle mass is increased. Along with this, IGF-1 levels will increase, as well, along with the different hypothalamus functions.
GHRP 2 Application:
GHRP-2 basically acts exactly like ghrelin. It can induce food consumption just like ghrelin and stimulate GH secretion, too. When infused, GHRP-2 makes the GH levels in the body increase a lot and it can induce cell cAMP secretion the way that GRF tends to, as well.
GHRP-2 as a Growth Hormone Secretagogue
GHRP-2 has been studied extensively for its utility as a growth hormone secretagogue (GHS). Scientists have discovered that the Growth Hormone Releasing Peptide-2 increases the natural production of growth hormone (GH). In the early 90’s, one of the most famous studies was performed and later published in 1997 in the Journal of Endocrinology and Metabolism. This study further exemplifies the theory that growth hormone releasing peptides (including Ipamorelin and GHRP-6) could help hormone deficient adults and children. Ever since these major scientific studies, GHRP-2 has been widely produced. With other scientific labs confirming the results from their studies, GHRP-2 can in fact work for those who lack the ability to make adequate human growth.

1-Boc-3-(cyanomethylene)azetidine CAS:1153949-11-1 LAB GRADE 98.5






Appearance:off-white solid

MOL File:1153949-11-1.mol

Application:Use as the pharma intermediates


4C-PVP 4cpvp crystal, manufactuer supply CAS NO.5537-17-7 CP >99%

  • ProName: 4C-PVP 4cpvp crystal
  • CasNo: 5537-17-7
  • Molecular Formula: C20H27FN2O3
  • Appearance: crystal
  • Application: researching of medicine
  • DeliveryTime: within 3 days after payment
  • PackAge: 1kg/Aluminum foil bag as customized
  • Port: shanghai shenzhen tianjin hongkong
  • ProductionCapacity: 1000 Kilogram/Month
  • Purity: 99%
  • Storage: Keep in dry and cool place
  • Transportation: Safe and fast delivery
  • LimitNum: 10 Gram
  • Related Substances: <0.5%
  • Residue on Ignition: 0.001
  • Heavy Metal: 0.001
  • Valid Period: 1 year
  • DeliveryTime: 5-8 days
  • PackAge: aluminous bag, kits

9-Amino-(9-deoxy)epi-dihydroquinine trihydrochloride Purified 99

9-Amino-(9-deoxy)epi-dihydroquinine trihydrochloride CAS No.     931098-91-8

Product Name:    9-Amino-(9-deoxy)epi-dihydroquinine trihydrochloride

CAS No:      931098-91-8

Synonyms:   9-Amino-(9-deoxy)epi-dihydroquinine trihydrochloride;(8α,9S)-10,11-Dihydro-6′-methoxycinchonan-9-amine trihydrochloride ;(8alpha,9S)-10,11-Dihydro-6'-methoxycinchonan-9-amine trihydrochloride 90%

MF:       C20H27N3O·3HCl

Purity ≥98%


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Shanghai Goyic Pharma. & Chem. Co., Ltd

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Tel: 86-21-50689757

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Quinine& derivatives

1.    Quinine, (R)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methanol              130-95-0

2.    9-Amino-(9-deoxy)epi-quinine trihydrochloride          168960-95-0

Dihydroquinine& derivatives

1.    Dihydroquinine,(R)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methanol    522-66-7

2.    9-Amino-(9-deoxy)epi-dihydroquinine trihydrochloride  931098-91-8

3     (DHQ)2PYR;Hydroquinine 2,5-diphenyl-4,6-pyrimidinediyl Diether 149820-65-5

Quinidine & derivatives

1.    Quinidine;(S)-(6-methoxyquinolin-4-yl)((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methanol     56-54-2

2.    9-Amino-(9-deoxy)epi- quinidine trihydrochloride     1391506-12-9

Dihydroquinidine& derivatives

1.    Dihydroquinidine;(S)-((1S,2R,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methanol 1435-55-8

2.    9-Amino-(9-deoxy)epi- dihydroquinidinetrihydrochloride  931098-92-9

3     (DHQD)2PYR; Hydroquinidine-2,5-diphenyl-4,6-pyrimidinediyl Diether 149725-81-5

Cinchonine& derivatives

1.    Cinchonine ;(S)-quinolin-4-yl((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methanol      118-10-5

2.    9-Amino-(9-deoxy)epi-Cinchonine trihydrochloride    168960-96-1

Dihydrocinchonine& derivatives

1.    Dihydrocinchonine ;(S)-((1S,2R,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methanol      485-65-4

2.    9-Amino-(9-deoxy)epi- Dihydrocinchonine trihydrochloride      354532-49-3

Cinchonidine& derivatives

1.    Cinchonidine;(R)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methanol       485-71-2

2.    9-Amino-(9-deoxy)epi- Cinchonidine trihydrochloride       850409-61-9

Dihydrocinchonidine & derivatives

1.    Dihydrocinchonidine; (R)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methanol  485-64-3

2.    9-Amino-(9-deoxy)epi-Dihydrocinchonidinetrihydrochloride

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